Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
Source | Last Updated |
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Alliance of Genome Resources | October 9, 2024 |
Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
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DOID:10286 | prostate carcinoma | HGNC:11246 | Homo sapiens (human) | 6692 | SPINT1 |
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DOID:10652 | Alzheimer's disease | HGNC:11246 | Homo sapiens (human) | 6692 | SPINT1 |
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DOID:5517 | stomach carcinoma | HGNC:11246 | Homo sapiens (human) | 6692 | SPINT1 |
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DOID:1612 | breast cancer | HGNC:11246 | Homo sapiens (human) | 6692 | SPINT1 |
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DOID:5082 | liver cirrhosis | HGNC:11246 | Homo sapiens (human) | 6692 | SPINT1 |
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DOID:8893 | psoriasis | HGNC:11246 | Homo sapiens (human) | 6692 | SPINT1 |
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DOID:2394 | ovarian cancer | HGNC:11246 | Homo sapiens (human) | 6692 | SPINT1 |
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DOID:299 | adenocarcinoma | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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DOID:0050700 | cardiomyopathy | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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DOID:3070 | high grade glioma | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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DOID:9970 | obesity | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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DOID:0110816 | hereditary spastic paraplegia 7 | HGNC:11237 | Homo sapiens (human) | 6687 | SPG7 |
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DOID:0110792 | hereditary spastic paraplegia 4 | HGNC:11233 | Homo sapiens (human) | 6683 | SPAST |
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DOID:2476 | hereditary spastic paraplegia | HGNC:11233 | Homo sapiens (human) | 6683 | SPAST |
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DOID:0110176 | Charcot-Marie-Tooth disease axonal type 2X | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
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DOID:0110764 | hereditary spastic paraplegia 11 | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
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DOID:0060197 | amyotrophic lateral sclerosis type 5 | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
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DOID:0050700 | cardiomyopathy | HGNC:11220 | Homo sapiens (human) | 8404 | SPARCL1 |
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DOID:856 | biotinidase deficiency | HGNC:1122 | Homo sapiens (human) | 686 | BTD |
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DOID:0110338 | osteogenesis imperfecta type 17 | HGNC:11219 | Homo sapiens (human) | 6678 | SPARC |
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DOID:5517 | stomach carcinoma | HGNC:11219 | Homo sapiens (human) | 6678 | SPARC |
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DOID:2871 | endometrial carcinoma | HGNC:11219 | Homo sapiens (human) | 6678 | SPARC |
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DOID:2152 | ovary epithelial cancer | HGNC:11219 | Homo sapiens (human) | 6678 | SPARC |
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DOID:11713 | diabetic angiopathy | HGNC:11219 | Homo sapiens (human) | 6678 | SPARC |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024